A self-organized 3-diethylaminopropyl-bearing glycol chitosan nanogel for tumor acidic pH targeting: In vitro evaluation

被引:59
作者
Oh, Nam Muk [1 ]
Oh, Kyung Taek [2 ]
Baik, Hye Jung [1 ]
Lee, Bo Reum [1 ]
Lee, A. Hyeong [1 ]
Youn, Yu Seok [3 ]
Lee, Eun Seong [1 ]
机构
[1] Catholic Univ Korea, Div Biotechnol, Bucheon Si 420743, Gyeonggi Do, South Korea
[2] Chung Ang Univ, Coll Pharm, Seoul 155756, South Korea
[3] Pusan Natl Univ, Coll Pharm, Pusan 609735, South Korea
关键词
pH-responsive nanogel; Glycol chitosan; 3-Diethylaminopropyl; Tumor extracellular pH; MULTIFUNCTIONAL POLYMERIC MICELLE; POORLY SOLUBLE DRUGS; MULTIDRUG-RESISTANCE; EXTRACELLULAR PH; DELIVERY; CANCER; NANOTECHNOLOGY; OPPORTUNITIES; TRANSPORTERS; EXPRESSION;
D O I
10.1016/j.colsurfb.2010.02.023
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this study, a novel pH-responsive nanogel composed of glycol chitosan (GCS) grafted with functional 3-diethylaminopropyl (DEAP) groups (denoted as GCS-g-DEAP hereafter) was fabricated. The GCS-g-DEAP was designed to have a self-assembled arrangement consisting of hydrophilic block (GCS) and hydrophobic block (DEAP) at physiological pH. As the pH decreased to tumor extracellular pH (pH(e)), the nanogel was destabilized due to the protonation of DEAP. The pH-responsive property of the nanogel at tumor extracellular pH (pH(e)) was characterized in drug-release kinetic studies. The release of doxorubicin (DOX) from DOX-loaded nanogels was significantly accelerated at lower pH values, which allowed for increased DOX uptake by non-small lung carcinoma A546 cells under a slightly acidic pH condition, as in tumor pH(e). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 126
页数:7
相关论文
共 28 条
[1]   A family of drug transporters: The multidrug resistance-associated proteins [J].
Borst, P ;
Evers, R ;
Kool, M ;
Wijnholds, J .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (16) :1295-1302
[2]  
Chaudhry A, 1999, CLIN CANCER RES, V5, P3385
[3]   Inner core segment design for drug delivery control of thermo-responsive polymeric micelles [J].
Chung, JE ;
Yokoyama, M ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 2000, 65 (1-2) :93-103
[4]   Expression of TRAIL and TRAIL receptors in normal and malignant tissues [J].
Daniels, RA ;
Turley, H ;
Kimberley, FC ;
Liu, XS ;
Mongkolsapaya, J ;
Ch'en, P ;
Xu, XN ;
Jin, BQ ;
Pezzella, F ;
Screaton, GR .
CELL RESEARCH, 2005, 15 (06) :430-438
[5]   Cancer nanotechnology: Opportunities and challenges [J].
Ferrari, M .
NATURE REVIEWS CANCER, 2005, 5 (03) :161-171
[6]   Mechanisms of cancer drug resistance [J].
Gottesman, MM .
ANNUAL REVIEW OF MEDICINE, 2002, 53 :615-627
[7]   Multidrug resistance in cancer: Role of ATP-dependent transporters [J].
Gottesman, MM ;
Fojo, T ;
Bates, SE .
NATURE REVIEWS CANCER, 2002, 2 (01) :48-58
[8]   P-glycoprotein and multidrug resistance [J].
Gottesman, MM ;
Pastan, I ;
Ambudkar, SV .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (05) :610-617
[9]   Preparation and characterization of poly(ethylene glycol)-g-chitosan with water- and organosolubility [J].
Hu, YQ ;
Jiang, HL ;
Xu, CN ;
Wang, YJ ;
Zhu, KJ .
CARBOHYDRATE POLYMERS, 2005, 61 (04) :472-479
[10]   Super pH-sensitive multifunctional polymeric micelle [J].
Lee, ES ;
Na, K ;
Bae, YH .
NANO LETTERS, 2005, 5 (02) :325-329